FDA device listing
NOVAPROBE 4K UHD CAMERA SYSTEM - UHDCAM 4K,NOVAPROBE HD CAMERA SYSTEM - HDCAM 1750,NOVAPROBE HD CAMERA SYSTEM - HDCAM…
FDA device listing 1992165353 · NovaProbe Inc.
Key facts
| Proprietary names | NOVAPROBE 4K UHD CAMERA SYSTEM - UHDCAM 4K,NOVAPROBE HD CAMERA SYSTEM - HDCAM 1750,NOVAPROBE HD CAMERA SYSTEM - HDCAM 3000 |
|---|---|
| Owner/operator | NovaProbe Inc. |
| Owner/operator number | 10043192 |
| Product codes | FWL |
| Device names | FWL - Camera, Cine, Endoscopic, Without Audio |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4160 |
| Review panels | General & Plastic Surgery |
| Registered establishments | NOVAPROBE INC. |
| Establishment registrations | 3010120217 |
| FEI numbers | 3010120217 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database